Juvenile onset Huntington's disease in an Omani child with asymptomatic, at risk parents.
作者信息
Scrimgeour E M, Koul R L, Chand P R, Tharakan J K, Frew C A
出版信息
J Med Genet. 1997 Aug;34(8):701. doi: 10.1136/jmg.34.8.701.
Abstract
摘要
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Juvenile onset Huntington's disease in an Omani child with asymptomatic, at risk parents.一名阿曼儿童患青少年型亨廷顿舞蹈症，其父母无症状但有患病风险。
J Med Genet. 1997 Aug;34(8):701. doi: 10.1136/jmg.34.8.701.
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引用本文的文献
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Huntington disease (chorea) in the middle East.中东地区的亨廷顿病（舞蹈症）
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本文引用的文献
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Molecular analysis of new mutations for Huntington's disease: intermediate alleles and sex of origin effects.亨廷顿舞蹈病新突变的分子分析：中间等位基因与起源性别效应
Nat Genet. 1993 Oct;5(2):174-9. doi: 10.1038/ng1093-174.
2
A worldwide study of the Huntington's disease mutation. The sensitivity and specificity of measuring CAG repeats.亨廷顿舞蹈症突变的全球研究。测量CAG重复序列的敏感性和特异性。
N Engl J Med. 1994 May 19;330(20):1401-6. doi: 10.1056/NEJM199405193302001.
3
Huntington's disease in two unrelated Arab kindreds and in an Afghani family resident in Saudi Arabia.两个不相关的阿拉伯家族以及居住在沙特阿拉伯的一个阿富汗家庭中的亨廷顿舞蹈症。
J Med Genet. 1994 Oct;31(10):819-20. doi: 10.1136/jmg.31.10.819.
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